glm_gp: Fit a Gamma-Poisson Generalized Linear Model

View source: R/glm_gp.R

glm_gpR Documentation

Fit a Gamma-Poisson Generalized Linear Model

Description

This function provides a simple to use interface to fit Gamma-Poisson generalized linear models. It works equally well for small scale (a single model) and large scale data (e.g. thousands of rows and columns, potentially stored on disk). The function automatically determines the appropriate size factors for each sample and efficiently finds the best overdispersion parameter for each gene.

Usage

glm_gp(
  data,
  design = ~1,
  col_data = NULL,
  reference_level = NULL,
  offset = 0,
  size_factors = c("normed_sum", "deconvolution", "poscounts", "ratio"),
  overdispersion = TRUE,
  overdispersion_shrinkage = TRUE,
  ridge_penalty = 0,
  do_cox_reid_adjustment = TRUE,
  subsample = FALSE,
  on_disk = NULL,
  use_assay = NULL,
  verbose = FALSE
)

Arguments

data

any matrix-like object (e.g. matrix, DelayedArray, HDF5Matrix) or anything that can be cast to a SummarizedExperiment (e.g. MSnSet, eSet etc.) with one column per sample and row per gene.

design

a specification of the experimental design used to fit the Gamma-Poisson GLM. It can be a model.matrix() with one row for each sample and one column for each coefficient.
Alternatively, design can be a formula. The entries in the formula can refer to global objects, columns in the col_data parameter, or the colData(data) of data if it is a SummarizedExperiment.
The third option is that design is a vector where each element specifies to which condition a sample belongs.
Default: design = ~ 1, which means that all samples are treated as if they belong to the same condition. Note that this is the fasted option.

col_data

a dataframe with one row for each sample in data. Default: NULL.

reference_level

a single string that specifies which level is used as reference when the model matrix is created. The reference level becomes the intercept and all other coefficients are calculated with respect to the reference_level. Default: NULL.

offset

Constant offset in the model in addition to log(size_factors). It can either be a single number, a vector of length ncol(data) or a matrix with the same dimensions as dim(data). Note that if data is a DelayedArray or HDF5Matrix, offset must be as well. Default: 0.

size_factors

in large scale experiments, each sample is typically of different size (for example different sequencing depths). A size factor is an internal mechanism of GLMs to correct for this effect.
size_factors is either a numeric vector with positive entries that has the same lengths as columns in the data that specifies the size factors that are used. Or it can be a string that species the method that is used to estimate the size factors (one of c("normed_sum", "deconvolution", "poscounts", "ratio")). Note that "normed_sum" and "poscounts" are fairly simple methods and can lead to suboptimal results. For the best performance on data with many zeros, I recommend to use size_factors = "deconvolution" which calls scran::calculateSumFactors(). However, you need to separately install the scran package from Bioconductor for this method to work. For small datasets common for bulk RNA-seq experiments, I recommend to use size_factors = "ratio", which uses the same procedure as DESeq2 and edgeR. Also note that size_factors = 1 and size_factors = FALSE are equivalent. If only a single gene is given, no size factor is estimated (ie. size_factors = 1). Default: "normed_sum".

overdispersion

the simplest count model is the Poisson model. However, the Poisson model assumes that variance = mean. For many applications this is too rigid and the Gamma-Poisson allows a more flexible mean-variance relation (variance = mean + mean^2 * overdispersion).
overdispersion can either be

  • a single boolean that indicates if an overdispersion is estimated for each gene.

  • a numeric vector of length nrow(data) fixing the overdispersion to those values.

  • the string "global" to indicate that one dispersion is fit across all genes.

Note that overdispersion = 0 and overdispersion = FALSE are equivalent and both reduce the Gamma-Poisson to the classical Poisson model. Default: TRUE.

overdispersion_shrinkage

the overdispersion can be difficult to estimate with few replicates. To improve the overdispersion estimates, we can share information across genes and shrink each individual overdispersion estimate towards a global overdispersion estimate. Empirical studies show however that the overdispersion varies based on the mean expression level (lower expression level => higher dispersion). If overdispersion_shrinkage = TRUE, a median trend of dispersion and expression level is fit and used to estimate the variances of a quasi Gamma Poisson model (Lund et al. 2012). Default: TRUE.

ridge_penalty

to avoid overfitting, we can penalize fits with large coefficient estimates. Instead of directly minimizing the deviance per gene (\sum dev(y_i, X_i b)), we will minimize \sum dev(y_i, X_i b) + N * \sum (penalty_p * b_p)^2.
ridge_penalty can be

  • a scalar in which case all parameters except the intercept are penalized.

  • a vector which has to have the same length as columns in the model matrix

  • a matrix with the same number of columns as columns in the model matrix. This gives maximum flexibility for expert users and allows for full Tikhonov regularization.

Default: ridge_penalty = 0, which is internally replaced with a small positive number for numerical stability.

do_cox_reid_adjustment

the classical maximum likelihood estimator of the overdisperion is biased towards small values. McCarthy et al. (2012) showed that it is preferable to optimize the Cox-Reid adjusted profile likelihood.
do_cox_reid_adjustment can be either be TRUE or FALSE to indicate if the adjustment is added during the optimization of the overdispersion parameter. Default: TRUE.

subsample

the estimation of the overdispersion is the slowest step when fitting a Gamma-Poisson GLM. For datasets with many samples, the estimation can be considerably sped up without loosing much precision by fitting the overdispersion only on a random subset of the samples. Default: FALSE which means that the data is not subsampled. If set to TRUE, at most 1,000 samples are considered. Otherwise the parameter just specifies the number of samples that are considered for each gene to estimate the overdispersion.

on_disk

a boolean that indicates if the dataset is loaded into memory or if it is kept on disk to reduce the memory usage. Processing in memory can be significantly faster than on disk. Default: NULL which means that the data is only processed in memory if data is an in-memory data structure.

use_assay

Specify which assay to use. Default: NULL, which means that if available 'counts' are used. Otherwise an error is thrown except if there is only a single assay.

verbose

a boolean that indicates if information about the individual steps are printed while fitting the GLM. Default: FALSE.

Details

The method follows the following steps:

  1. The size factors are estimated.
    If size_factors = "normed_sum", the column-sum for each cell is calculated and the resulting size factors are normalized so that their geometric mean is 1. If size_factors = "poscounts", a slightly adapted version of the procedure proposed by Anders and Huber (2010) in equation (5) is used. To handle the large number of zeros the geometric means are calculated for Y + 0.5 and ignored during the calculation of the median. Columns with all zeros get a default size factor of 0.001. If size_factors = "deconvolution", the method scran::calculateSumFactors() is called. If size_factors = "ratio", the unmodified procedure from Anders and Huber (2010) in equation (5) is used.

  2. The dispersion estimates are initialized based on the moments of each row of Y.

  3. The coefficients of the model are estimated.
    If all samples belong to the same condition (i.e. design = ~ 1), the betas are estimated using a quick Newton-Raphson algorithm. This is similar to the behavior of edgeR. For more complex designs, the general Fisher-scoring algorithm is used. Here, the code is based on a fork of the internal function fitBeta() from DESeq2. It does however contain some modification to make the fit more robust and faster.

  4. The mean for each gene and sample is calculate.
    Note that this step can be very IO intensive if data is or contains a DelayedArray.

  5. The overdispersion is estimated.
    The classical method for estimating the overdispersion for each gene is to maximize the Gamma-Poisson log-likelihood by iterating over each count and summing the the corresponding log-likelihood. It is however, much more efficient for genes with many small counts to work on the contingency table of the counts. Originally, this approach had already been used by Anscombe (1950). In this package, I have implemented an extension of their method that can handle general offsets.
    See also overdispersion_mle().

  6. The beta coefficients are estimated once more with the updated overdispersion estimates

  7. The mean for each gene and sample is calculated again.

This method can handle not just in memory data, but also data stored on disk. This is essential for large scale datasets with thousands of samples, as they sometimes encountered in modern single-cell RNA-seq analysis. glmGamPoi relies on the DelayedArray and beachmat package to efficiently implement the access to the on-disk data.

Value

The method returns a list with the following elements:

Beta

a matrix with dimensions ⁠nrow(data) x n_coefficients⁠ where n_coefficients is based on the design argument. It contains the estimated coefficients for each gene.

overdispersions

a vector with length nrow(data). The overdispersion parameter for each gene. It describes how much more the counts vary than one would expect according to the Poisson model.

overdispersion_shrinkage_list

a list with additional information from the quasi-likelihood shrinkage. For details see overdispersion_shrinkage().

deviances

a vector with the deviance of the fit for each row. The deviance is a measure how well the data is fit by the model. A smaller deviance means a better fit.

Mu

a matrix with the same dimensions as dim(data). If the calculation happened on disk, than Mu is a HDF5Matrix. It contains the estimated mean value for each gene and sample.

size_factors

a vector with length ncol(data). The size factors are the inferred correction factors for different sizes of each sample. They are also sometimes called the exposure factor.

Offset

a matrix with the same dimensions as dim(data). If the calculation happened on disk, than Offset is a HDF5Matrix. It contains the log(size_factors) + offset from the function call.

data

a SummarizedExperiment that contains the input counts and the col_data

model_matrix

a matrix with dimensions ⁠ncol(data) x n_coefficients⁠. It is build based on the design argument.

design_formula

the formula that used to fit the model, or NULL otherwise

ridge_penalty

a vector with the specification of the ridge penalty.

References

  • McCarthy, D. J., Chen, Y., & Smyth, G. K. (2012). Differential expression analysis of multifactor RNA-Seq experiments with respect to biological variation. Nucleic Acids Research, 40(10), 4288–4297. https://doi.org/10.1093/nar/gks042.

  • Anders Simon, & Huber Wolfgang. (2010). Differential expression analysis for sequence count data. Genome Biology. https://doi.org/10.1016/j.jcf.2018.05.006.

  • Love, M. I., Huber, W., & Anders, S. (2014). Moderated estimation of fold change and dispersion for RNA-seq data with DESeq2. Genome Biology, 15(12), 550. https://doi.org/10.1186/s13059-014-0550-8.

  • Robinson, M. D., McCarthy, D. J., & Smyth, G. K. (2009). edgeR: A Bioconductor package for differential expression analysis of digital gene expression data. Bioinformatics, 26(1), 139–140. https://doi.org/10.1093/bioinformatics/btp616.

  • Lun ATL, Pagès H, Smith ML (2018). “beachmat: A Bioconductor C++ API for accessing high-throughput biological data from a variety of R matrix types.” PLoS Comput. Biol., 14(5), e1006135. doi: 10.1371/journal.pcbi.1006135..

  • Lund, S. P., Nettleton, D., McCarthy, D. J., & Smyth, G. K. (2012). Detecting differential expression in RNA-sequence data using quasi-likelihood with shrunken dispersion estimates. Statistical Applications in Genetics and Molecular Biology, 11(5). https://doi.org/10.1515/1544-6115.1826.

  • Lun ATL, Bach K and Marioni JC (2016). Pooling across cells to normalize single-cell RNA sequencing data with many zero counts. Genome Biol. 17:75 https://doi.org/10.1186/s13059-016-0947-7

See Also

overdispersion_mle() and overdispersion_shrinkage() for the internal functions that do the work. For differential expression analysis, see test_de().

Examples

 set.seed(1)
 # The simplest example
 y <- rnbinom(n = 10, mu = 3, size = 1/2.4)
 c(glm_gp(y, size_factors = FALSE))

 # Fitting a whole matrix
 model_matrix <- cbind(1, rnorm(5))
 true_Beta <- cbind(rnorm(n = 30), rnorm(n = 30, mean = 3))
 sf <- exp(rnorm(n = 5, mean = 0.7))
 model_matrix
 Y <- matrix(rnbinom(n = 30 * 5, mu = sf * exp(true_Beta %*% t(model_matrix)), size = 1/2.4),
             nrow = 30, ncol = 5)

 fit <- glm_gp(Y, design = model_matrix, size_factors = sf, verbose = TRUE)
 summary(fit)

 # Fitting a model with covariates
 data <- data.frame(fav_food = sample(c("apple", "banana", "cherry"), size = 50, replace = TRUE),
 city = sample(c("heidelberg", "paris", "new york"), size = 50, replace = TRUE),
 age = rnorm(n = 50, mean = 40, sd = 15))
 Y <- matrix(rnbinom(n = 100 * 50, mu = 3, size = 1/3.1), nrow = 100, ncol = 50)
 fit <- glm_gp(Y, design = ~ fav_food + city + age, col_data = data)
 summary(fit)

 # Specify 'ridge_penalty' to penalize extreme Beta coefficients
 fit_reg <- glm_gp(Y, design = ~ fav_food + city + age, col_data = data, ridge_penalty = 1.5)
 summary(fit_reg)



const-ae/glmGamPoi documentation built on July 25, 2024, 10:22 p.m.